GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Database Last Updated
Alliance of Genome Resources February 28, 2024
DisGeNET February 14, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Disease ID Disease Name Gene Symbol Gene ID ▲
  • autosomal recessive limb-girdle muscular dystrophy type 2O
  • congenital muscular dystrophy-dystroglycanopathy type A3
  • muscular dystrophy-dystroglycanopathy type B3
  • paroxysmal nocturnal hemoglobinuria
  • multiple congenital anomalies-hypotonia-seizures syndrome 2
  • autosomal recessive congenital ichthyosis 4B
  • congenital muscular dystrophy-dystroglycanopathy type A13
  • macular corneal dystrophy
  • multiple sclerosis
  • cortisone reductase deficiency
Displaying entries 151 - 160 of 1885 in total

International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01